44608-8

LOINC 2.82

KCNQ1 gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal

KCNQ1 gene Mut Tested Bld/T

Component

  • KCNQ1 gene mutations tested for

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • ATFB1; ATFB3; Blood; Gene mut tested; Genetics; Heredity; Heritable; Identity or presence; Inherited; JLNS1; KCNA8; KCNA9; KCNQ10T1; Kv1.9; Kv7.1; KVLQT1; Long (electrocardiographic) QT syndrome, Ward-Romano syndrome 1; LQT; LQT1; LQTS; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Tested; Mutation; Muts; Nominal; PCR; Point in time; potassium channel, voltage gated KQT-like subfamily Q, member 1; Potassium voltage-gated channel, KQT-like subfamily, member 1; Random; RWS; SQT2; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue; WRS

Index terms

  • ATFB1
  • ATFB3
  • Blood
  • Gene mut tested
  • Genetics
  • Heredity
  • Heritable
  • Identity or presence
  • Inherited
  • JLNS1
  • KCNA8
  • KCNA9
  • KCNQ10T1
  • Kv1.9
  • Kv7.1
  • KVLQT1
  • Long (electrocardiographic) QT syndrome, Ward-Romano syndrome 1
  • LQT
  • LQT1
  • LQTS
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mut Tested
  • Mutation
  • Muts
  • Nominal
  • PCR
  • Point in time
  • potassium channel, voltage gated KQT-like subfamily Q, member 1
  • Potassium voltage-gated channel, KQT-like subfamily, member 1
  • Random
  • RWS
  • SQT2
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood

2 further terms